水稻种植对黑土微生物生物量和碳源代谢功能的影响

采用磷脂脂肪酸方法和Biolog-ECO微平板检测法,以吉林省长春市双阳区农业技术推广站实验区的土壤为对象,研究了水稻种植对黑土微生物生态结构和功能的影响.结果表明空地中有机质含量最高,其次为田间土,根际土中有机质含量最低;在夏季的样品中有机质含量最高,土壤中全氮的变化趋势与土壤有机质比较相似.土壤微生物群落功能多样性指数则表现为夏季显著高于秋季和春季,春、秋两季差异不明显,冬季最低,空地中微生物群落的Shannon-Wiener指数和Pielou均匀度指数高于田间和根际.全部样品微生物生长步入稳定期时间和碳源的颜色平均变化率变化范围不同,时间分别为216、192、216、120 h,范围分别为0.52~0.84、0.82~1.28、0.40~0.84、0.05~0.48,表明春秋季微生物步入稳定期和对碳源的代谢量比较相似,夏季最大,冬季最小.研究结果为科学评价典型水稻种植黑土区土壤生境质量退化与恢复过程中微生物特征的变化提供参考.     

3种典型消毒副产物对细菌抗生素抗性的影响

本文研究了消毒副产物对细菌抗生素抗性的作用.分别选取三卤甲烷类(THMs)、卤乙酸类(HAAs)以及醛类消毒副产物中典型物质一氯二溴甲烷(CDBM)、碘乙酸(IAA)和水合三氯乙醛(CH),研究了细菌经消毒副产物染毒之后,对多种抗生素的抗性变化情况.结果发现,3种消毒副产物均可以诱导野生型铜绿假单胞菌提高对5种受试抗生素的抗性,提高作用IAACHCDBM.IAA对多重抗性也具有一定的提高作用.野生型大肠杆菌的抗生素抗性同样能够被DBPs诱导提高,说明DBPs对抗性的影响具有普遍性.其作用机制可能是DBPs通过氧化胁迫机制诱导细菌发生突变,进而提高细菌抗生素抗性.本研究表明饮用水系统中部分细菌抗生素抗性的获得可能与消毒副产物有关;除毒理学风险外,消毒副产物的流行病学风险同样不容忽视.     

“The Kesterson effect”

Hypothesized to be derived from Cretaceous marine sedimentary rocks, selenium contamination of the Kesterson National Wildlife Refuge is traced through irrigation drainage to the source bedrock of the California Coast Ranges. This biogeochemical pathway of selenium is defined here as the “Kesterson effect.” At the refuge ponds, this effect culminated in 1983 in a 64% rate of deformity and death of embryos and hatchlings of wild aquatic birds. From the previous companion paper on irrigation drainage, the Kesterson effect has been implicated in nine of 11 reconnaissance areas studied in the western United States. Deformities have resulted in at least five of these sites. Climatic, geologic, hydrologic, and soil conditions in these reconnaissance areas are similar to those in the area surrounding Kesterson National Wildlife Refuge in the west-central San Joaquin Valley of California. In California, selenium, as selenate, was ultimately found weathered with sulfur from marine sources in soluble sodium and magnesium sulfate salts, which are concentrated by evaporation on farmland soils. The Se, mobilized by irrigation drainage, is bioaccumulated to toxic levels in refuge wetland ponds that are located mainly in hydrologically closed basins and thus act as concentrating disposal points. The depositional environment of the ponds may be similar to that of the nutrient-rich continental shelf edge and slope in which Cretaceous, Eocene, and Miocene sediments found to be seleniferous in the California Coast Ranges were deposited. Bioaccumulation may be therefore a primary mechanism of selenium enrichment in ancient sediments in addition to that of the formerly suggested Cretaceous volcanic pathway.     

Application of recombinant gene technology for production of polyhydroxyalkanoic acids: Biosynthesis of poly(4-hydroxybutyric acid) homopolyester

Screening of a large number of bacteria revealed several strains, which utilize 1,4-butanediol and/or 4-hydroxybutyric acid (4HB) as a carbon source for growth and for synthesis of polyhydroxyalkanoic acids (PHA) containing 4HB as one constituent among others (mostly 3-hydroxybutyric acid). However, none of the wild-type strains investigated in this study was able to produce a homopolyester consisting solely of 4HB. Only several poly(3-hydroxybutyric acid)-leaky mutants ofAlcaligenes eutrophus strain JMP222 synthesized poly(4HB) homopolyester, which amounted to approximately 10% (w/w) of the cellular dry matter. If the PHA synthase structural gene ofA. eutrophus strain H16 was expressed in these mutants, the amount of poly(4HB) was increased to approximately 30% (w/w). The occurrence of poly(4HB) was demonstrated by gas chromatographic as well as¹H and¹³C nuclear magnetic resonance spectroscopic analysis.Paper presented at the Bio/Environmentally Degradable Polymer Society—Second National Meeting, August 19–21, 1993, Chicago, Illinois.     

Laboratory-scale chlorination to estimate the levels of halogenated DBPs in full-scale distribution systems

Occurrence of halogenated disinfection by-products (DBPs) (trihalomethanes –THMs– and haloacetic acids –HAAs–) in the waters of two utilities in Quebec City (Canada) was investigated using two approaches: experimental chlorination studies and full-scale sampling within distribution systems. Experimental studies were designed to reproduce treatment plant and distribution system conditions (chlorine dose, water temperature, pH and water residence time). Differences in halogenated DBPs in the two distribution systems under study were significant and comparable to those observed in experimental laboratory studies. For the waters of both utilities, chlorination studies better reproduced the occurrence of halogenated DBPs in points of the distribution system located near the treatment plant (low residence time of water) than in other points. Multivariate regression models for THMs, HAAs and their species were developed using the data from experimental studies in order to predict halogenated DBP levels measured in the distribution system. Models were all statistically significant, but showed low ability to predict full-scale halogenated DBPs, particularly in points located at distribution system extremities. Specifically, experimental chlorination-based models are not able to simulate the decrease of HAA levels. Results of this research suggest that the use of experimental data to predict halogenated DBP levels in full-scale distribution systems – for operational, regulatory and epidemiological purposes – must be done with caution.     

腐殖酸-海泡石复合钝化剂的制备及其对Cd污染土壤的修复

对海泡石进行热改性,以腐殖酸和海泡石为原料,制备了腐殖酸-海泡石复合钝化剂。采用BCR形态分析法研究了复合钝化剂对镉污染土壤的钝化效果。结果表明,制备复合钝化剂的最佳工艺条件为：腐殖酸与海泡石质量比2∶1,氢氧化钠质量浓度0.04 g/mL,热反应时间40 min,热反应温度80 ℃。复合钝化剂的最佳添加量为7%（w）,培养3 d后,钝化效率达46.87%,土壤pH升高至7.02,活稳比降低为0.65,土壤中镉的释放风险显著降低。复合钝化剂修复镉污染土壤时,会促使活性态镉向稳定态镉转化,使镉在土壤中的稳定性提高。     

郑州市PM2.5中有机酸的污染特征、来源解析及二次生成

大气颗粒物中的有机酸广泛参与大气中的各种物理化学反应,对二次有机气溶胶和霾的形成贡献极大,因此分析颗粒物中有机酸的浓度分布特征、评估其污染来源、探究其二次生成,对深入研究有机气溶胶及其二次转化具有重要意义.在郑州市不同季节采集大气细颗粒物（PM_2.5）样品,识别并定量二元酸类、脂肪酸类和树脂酸类有机酸共30种,探究其浓度分布特征、季节变化、来源贡献及二次生成.定量的二元酸类以丙二酸（di-C₃）和琥珀酸（di-C₄）含量最为丰富,并且表现出明显的季节变化特征：夏季 > 秋季 > 冬季 > 春季;脂肪酸类表现出明显的双峰优势,以棕榈酸和硬脂酸（C₁₈）最为丰富,季节变化特征为冬季最高,春季最低.利用主成分分析结合多元线性回归（MLR）方法对郑州市PM_2.5中的有机酸进行来源解析,结果表明,35%的有机酸来自于燃烧源和交通源,24%来自于烹饪源、23%来自于二次生成以及17%来自于天然源.利用标记物种的比值（如di-C₃ /di-C₄、F/M和C_18：1 /C₁₈）探究有机气溶胶二次形成及其老化过程.结果表明,夏季光化学反应剧烈,有机气溶胶老化或二次生产比例较高,冬季光化学反应较弱,有机气溶胶老化程度较低.采用相关性分析与MLR相结合的方法,量化了气相氧化和液相氧化对二元酸形成的相对贡献,气相氧化在采样过程中起主导作用,占比为58%,特别是夏季,占总二次转化的61%.     

高铁酸钾预处理强化污泥破解及厌氧产酸

在序批式污泥厌氧反应器中探究了高铁酸钾对污泥破解及厌氧产酸的影响。实验结果表明高铁酸钾对污泥具有较强的破解性,当高铁酸钾的质量浓度由0 mg/L增加至16 mg/L时,溶解性COD与总COD的比值由6.2%升至35.6%。同时污泥液相中溶解性蛋白质的质量浓度由561 mg/L增加至1 365 mg/L。高铁酸钾的浓度与挥发性悬浮固体(VSS)的减量具有一定的线性关系。当高铁酸钾的质量浓度为8 mg/L时,污泥厌氧产挥发性脂肪酸最大,并且最大值为895 mg/L,其浓度是空白组2.56倍。     

累托石/腐殖酸微球的制备及其对Cr(Ⅵ)的吸附研究

采用累托石（REC）、腐殖酸（HA）等材料制备微球状吸附剂,考察了累托石、腐殖酸、聚乙烯醇（PVA）、海藻酸钠（SA）、氯化钙等材料的用量对制得的微球吸附性能的影响,通过正交试验确定了微球的最佳制备条件,还考察了微球用量、振荡时间和溶液pH值等因素对微球吸附去除水中Cr(VI)效果的影响。结果表明,采用累托石、腐殖酸、聚乙烯醇等材料可制得高效去除水中六价铬离子的微球状吸附剂,微球的最佳制备条件为：REC 1%,HA 4%,PVA 7%,SA 0.1%,CaCl₂ 0.5%。制得的累托石/腐殖酸微球孔系发达,吸附性能良好。在温度30℃,微球用量0.02 g/mL,振荡时间为2.5 h,pH值为1的条件下,微球对Cr(VI)的吸附效率可达98%以上。